Results
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CDKL5 protein substitution therapy rescues neurological phenotypes of a mouse model of CDKL5 disorder. [electronic resource] by
- Trazzi, Stefania
- De Franceschi, Marianna
- Fuchs, Claudia
- Bastianini, Stefano
- Viggiano, Rocchina
- Lupori, Leonardo
- Mazziotti, Raffaele
- Medici, Giorgio
- Lo Martire, Viviana
- Ren, Elisa
- Rimondini, Roberto
- Zoccoli, Giovanna
- Bartesaghi, Renata
- Pizzorusso, Tommaso
- Ciani, Elisabetta
Producer: 20190211
In:
Human molecular genetics vol. 27
Availability: No items available.
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